) The Molecular and Structural Biology Program brings together 23 outstanding investigators representing 10 departments, 3 UCHSC Schools (Medicine, Pharmacy, and the Graduate school), and 2 sister institutions (UCHSC & CU-Boulder). The scientific and programmatic goals of the Program are to elucidate key fundamental processes involved in cancer biology and to expand the molecular structure component of the Program, respectively. Our tremendous success in developing a Structural Biology initiative has broadened our Program into cutting-edge areas of basic science. The Program has been re-organized and members are now divided into three focal points of strength: Nucleic Acid Metabolism, Gene Transcription and Molecular Structure. This very well funded group of investigators ($6.3 million; direct costs) has provided key insights into molecular mechanisms regulating: DNA replication, repair, and re-arrangements; RNA trans-splicing and mRNA processing; stage-, cell- and signal-specific gene transcription; and in elucidating the chemical structures of DNA, RNA, protein and drug molecules. During the past five years our Program has had dramatic increases in total support (23%), NCI support (537%), and other Cancer Support (254%), showing remarkable progress. Additionally, members have published more than 200 reports in highly respected journals, underscoring the national prominence of Program faculty. Program members interact via several mechanisms, including monthly seminars, annual retreat, annual regional topical meetings, and annual mini-symposium. These formal mechanisms of interaction provide multiple opportunities for exchange of information and collaborative efforts. The Program makes heavy use of the DNA Sequencing, Tissue Culture/Monoclonal Antibody, Protein Chemistry and Flow Cytometry Cores. Our future plans are to further develop the Molecular Structure group, particularly in the area of proteomics, and to provide critical insights into the molecular mechanisms by which aberrations of the DNA replication machinery, transcription apparatus, and RNA processing components lead to cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA046934-14
Application #
6488560
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
1988-03-01
Project End
2006-01-31
Budget Start
Budget End
Support Year
14
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Type
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Tuttle, Kathryn D; Krovi, S Harsha; Zhang, Jingjing et al. (2018) TCR signal strength controls thymic differentiation of iNKT cell subsets. Nat Commun 9:2650
Keysar, Stephen B; Eagles, Justin R; Miller, Bettina et al. (2018) Salivary Gland Cancer Patient-Derived Xenografts Enable Characterization of Cancer Stem Cells and New Gene Events Associated with Tumor Progression. Clin Cancer Res 24:2935-2943
Salmon, Loïc; Stull, Frederick; Sayle, Sabrina et al. (2018) The Mechanism of HdeA Unfolding and Chaperone Activation. J Mol Biol 430:33-40
Kleczko, Emily K; Heasley, Lynn E (2018) Mechanisms of rapid cancer cell reprogramming initiated by targeted receptor tyrosine kinase inhibitors and inherent therapeutic vulnerabilities. Mol Cancer 17:60
Steckelberg, Anna-Lena; Akiyama, Benjamin M; Costantino, David A et al. (2018) A folded viral noncoding RNA blocks host cell exoribonucleases through a conformationally dynamic RNA structure. Proc Natl Acad Sci U S A 115:6404-6409
Pilling, Amanda B; Kim, Jihye; Estrada-Bernal, Adriana et al. (2018) ALK is a critical regulator of the MYC-signaling axis in ALK positive lung cancer. Oncotarget 9:8823-8835
Antonioli, Alexandra H; White, Janice; Crawford, Frances et al. (2018) Modulation of the Alternative Pathway of Complement by Murine Factor H-Related Proteins. J Immunol 200:316-326
Boswell, Zachary K; Rahman, Samiur; Canny, Marella D et al. (2018) A dynamic allosteric pathway underlies Rad50 ABC ATPase function in DNA repair. Sci Rep 8:1639
Fitzwalter, Brent E; Towers, Christina G; Sullivan, Kelly D et al. (2018) Autophagy Inhibition Mediates Apoptosis Sensitization in Cancer Therapy by Relieving FOXO3a Turnover. Dev Cell 44:555-565.e3
Duex, Jason E; Swain, Kalin E; Dancik, Garrett M et al. (2018) Functional Impact of Chromatin Remodeling Gene Mutations and Predictive Signature for Therapeutic Response in Bladder Cancer. Mol Cancer Res 16:69-77

Showing the most recent 10 out of 1634 publications